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Transition to ISO 15189 : 2012 for Cytopathology Laboratories Part 2: Technical Requirements

Author

Listed:
  • Eleftherios Vavoulidis

    (Medical School, Aristotle University of Thessaloniki and Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece)

  • Stavros Archondakis

    (401 General Military Hospital of Athens, Athens, Greece)

  • Maria Nasioutziki

    (Medical School, Aristotle University of Thessaloniki and Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece)

  • Ourania Oustambasidou

    (401 General Military Hospital of Athens, Athens, Greece)

  • Angelos Daniilidis

    (Medical School, Aristotle University of Thessaloniki and Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece)

  • Konstantinos Dinas

    (Medical School, Aristotle University of Thessaloniki and Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece)

  • Aristotelis Loufopoulos

    (Medical School, Aristotle University of Thessaloniki and Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece)

Abstract

Modern diagnostic medical laboratories personnel should be an ideal combination of highly qualified scientists and technologists who use innovative analytical equipment to provide high quality diagnostic services to mankind. A well-designed and a well-implemented Quality Management System (QMS) according to the ISO 15189 requirements is regarded as a prerequisite that will ensure that a cytopathology laboratory is capable enough to provide precise and credible results. The authors present their knowledge on the implementation of such a QMS in cytopathology laboratories and emphasize the most crucial technical parameters that should be considered when advancing from ISO 15189:2007 to the latest ISO 15189:2012. Furthermore, helpful advice and pointers that could accommodate relative transition are included. Finally, potential issues related to the laboratory's implementation of ISO 15189:2012 and a mobile technology application for better personnel management are also depicted.

Suggested Citation

  • Eleftherios Vavoulidis & Stavros Archondakis & Maria Nasioutziki & Ourania Oustambasidou & Angelos Daniilidis & Konstantinos Dinas & Aristotelis Loufopoulos, 2016. "Transition to ISO 15189 : 2012 for Cytopathology Laboratories Part 2: Technical Requirements," International Journal of Reliable and Quality E-Healthcare (IJRQEH), IGI Global, vol. 5(3), pages 22-41, July.
    • Handle: RePEc:igg:jrqeh0:v:5:y:2016:i:3:p:22-41
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